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Author Topic: hi new home dialysis  (Read 2324 times)
mike lane
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« on: November 14, 2010, 11:45:00 AM »
hi my name is Michael lane I'm been on dailysis, for a year and a half still sating to get on the kidney list maybe next year, i am single i got one daughter 20 living with me don't get out much except doctors app, i could use a Friend to talk to someone else going through home dailysis, thanks ???
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boswife
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us and fam easter 2013
« Reply #1 on: November 14, 2010, 06:11:31 PM »
welcome mike lane  :welcomesign;  I think you'll find a very friendly place here to talk and ask questions.  Theres off topic section too so thats always fun.  I even think theres a chat board but im not sure as i've never checked that out. We are going to be starting our training with NxStage soon, so at least i'll know what im talking about if you ask questions..  Hope you enjoy it here, i sure do!
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im a california wife and cargiver to my hubby
He started dialysis April 09
We thank God for every day we are blessed to have together.
november 2010, patiently (ha!) waiting our turn for NxStage training
January 14,2011 home with NxStage
MooseMom
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« Reply #2 on: November 14, 2010, 06:47:25 PM »
Hiya!  I'm not on D yet, but when it's my time, I plan to do it at home.  There are plenty of people on this forum who do home D, and they would be pleased to speak to you more about it.  There are also members who have been on D in-clinic but are looking to transition to home hemo or PD, so anything you would have to say on the subject would be welcomed, I'm sure.  Thanks for joining our community!
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"Eggs are so inadequate, don't you think?  I mean, they ought to be able to become anything, but instead you always get a chicken.  Or a duck.  Or whatever they're programmed to be.  You never get anything interesting, like regret, or the middle of last week."
Bruno
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TOFF (typical old Fart)
« Reply #3 on: November 14, 2010, 07:38:55 PM »
Hi Mike, welcome...there are plenty here on home HD...I'm one of them.
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Desert Dancer
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« Reply #4 on: November 14, 2010, 11:22:53 PM »
Hi, Mike and  :welcomesign;

I'm on home dialysis, too; what type of home dialysis do you do? I've only just finished training on a Fresenius machine and I do nocturnal hemo every other night. So far it's really working out great.
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August 1980: Diagnosed with Familial Juvenile Hyperurecemic Nephropathy (FJHN)
8.22.10:   Began dialysis through central venous catheter
8.25.10:   AV fistula created
9.28.10:   Began training for Home Nocturnal Hemodialysis on a Fresenius Baby K
10.21.10: Began creating buttonholes with 15ga needles
11.13.10: Our first nocturnal home treatment!

Good health is just the slowest possible rate at which you can die.

The glass is neither half-full nor half-empty. The glass is just twice as large as it needs to be.

The early bird may get the worm but the second mouse gets the cheese.
mike lane
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« Reply #5 on: November 15, 2010, 06:09:30 AM »
Quote from: Desert Dancer on November 14, 2010, 11:22:53 PM
Hi, Mike and  :welcomesign;hi dessert dancer I'm a cowboy up dancer when i get out my dailysis is OK except have to do it every 6 hours and not really getting to go on long trip's anymore i think my biggest problem is trying to get woman from dropping me after i tell them I'm on dailysis i allway tell them before we date or anything they all just stop galling or tell me i shouldn't have told them before we dated, what do you think I'm doing wrong? anyway you said you do he-mo dialysis is it hard on you how long at night are you on it i don't use the machine i try ed it but it didn't drain me the right way as manual so i do all manual exchange i like have control over that and i don't have to worry if the power goes out thanks for talking to me thanks

I'm on home dialysis, too; what type of home dialysis do you do? I've only just finished training on a Fresno's machine and I do nocturnal hemo every other night. So far it's really working out great.
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Rerun
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« Reply #6 on: November 15, 2010, 07:03:05 AM »
Hi Michael and welcome to IHD.  I'm so glad you found us.  I volunteer a few hours a week to keep myself from going crazy. 

This site is great.  I hope you come back often.

Rerun, Moderator       :welcomesign;
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peleroja
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I have 16 hats, all the same style!
« Reply #7 on: November 15, 2010, 07:37:18 AM »
Hi, Michael, and welcome to the group.  What kind of home dialysis?  I've been on PD for 7 years.  Tons of information and friends here.  Glad you joined!
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rsudock
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will of the healthy makes up the fate of the sick.
« Reply #8 on: November 15, 2010, 05:15:59 PM »
welcome!!!!
xo
R
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Born with autosomal recessive polycystic kidney disease
1995 - AV Fistula placed
Dec 7, 1999 cadaver transplant saved me from childhood dialysis!
10 transplant years = spleenectomy, gall bladder removed, liver biopsy, bone marrow aspiration.
July 27, 2010 Started dialysis for the first time ever.
June 21, 2011 2nd kidney nonrelated living donor
September 2013 Liver Cancer tumor.
October 2013 Ablation of liver tumor.
Now scans every 3 months to watch for new tumors.
Now Status 7 on the wait list for a liver.
How about another decade of solid health?
chook
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Born to be a Granma!
« Reply #9 on: November 15, 2010, 05:49:37 PM »
 :welcomesign;
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Diagnosed PKD 1967, age 8
Commenced PD June 2010
Commenced APD July 2010
Transplant March 2011 - so lucky!
"To strive, to seek, to find...and not to yield!"
Jean
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« Reply #10 on: November 16, 2010, 12:45:11 AM »
   :welcomesign; 
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One day at a time, thats all I can do.
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